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Can a 12-Week Supervised Program Improve Life with Sleep Apnea? A Study of Short- and Long-Term Benefits

Short-term effect of 12-week Comprehensive Supervised Intervention Program (SIP) on functioning of Individuals with Obstructive Sleep Apnea based on ICF Domains: 1-Year Follow-Up Experimental Study - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/02/0105018
Enrollment
100
Registered
2026-02-27
Start date
Unknown
Completion date
Unknown
Last updated
2026-03-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: J988- Other specified respiratory disorders

Interventions

Intervention1: Comprehensive Supervised Intervention Program: Participants in the intervention group will undergo a 12-week Comprehensive Supervised Intervention Program (SIP) conducted under physioth

Sponsors

MGM Medical college and hospital
Lead Sponsor
MGM Medical college and Hospital
Collaborator
MGM School of Physiotherapy
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: Adults aged 30 60 years. Diagnosed with moderate-to-severe obstructive sleep apnea with an AHI more than or equal to 15 events per hour. Not currently involved in any structured exercise program. Able to provide informed consent

Exclusion criteria

Exclusion criteria: Presence of significant comorbidities such as advanced cardiovascular disease or uncontrolled hypertension. Previous surgical intervention for OSA. Use of supplemental oxygen or other respiratory aids beyond CPAP. Cognitive impairment MoCA score less than 24

Design outcomes

Primary

MeasureTime frame
Primary Outcome Measures: 1. Sleep Apnea Quality of Life Index (SAQLI). 2. Montreal Cognitive Assessment (MoCA) score. Secondary Outcome Measures: 1. Changes in Apnea-Hypopnea Index (AHI) and other sleep parameters through polysomnography. 2. Oxygen saturation 3. Pittsburgh sleep quality index 4. Epworth Sleepiness Scale (ESS)Timepoint: Primary Outcome Measures: 1. Sleep Apnea Quality of Life Index (SAQLI). 2. Montreal Cognitive Assessment (MoCA) score. Secondary Outcome Measures: 1. Changes in Apnea-Hypopnea Index (AHI) and other sleep parameters through polysomnography. 2. Oxygen saturation 3. Pittsburgh sleep quality index 4. Epworth Sleepiness Scale (ESS)—

Secondary

MeasureTime frame
1. Changes in Apnea-Hypopnea Index (AHI) and other sleep parameters through polysomnography. 2. Oxygen saturation 3. Pittsburgh sleep quality index 4. Epworth Sleepiness Scale (ESS)Timepoint: 1. Primary outcome measures will be evaluated at baseline, 12 weeks, 12 month post intervention—

Countries

India

Contacts

Public ContactSantosh P Dobhal

MGM Institute of Health Sciences-MGM School of Physiotherapy School of Physiotherapy

ptsantosh07@gmail.com9923401079

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Apr 4, 2026